UMLS Hierarchy Tracer (Ancestors & Descendants)

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Target Concept: Genetic Variation (C0042333)

Ancestor Paths (Parents/Root)

Ancestor Path 1 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Phenomena and Processes (MeSH Category) CUI: C2930671 / Source: MSH
  6. Genetic Phenomena CUI: C2350469 / Source: MSH
  7. Genetic Variation (START) CUI: C0042333 / Source: MSH

Descendant Paths (Children/Leaves)

Descendant Path 1 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Antibody Diversity CUI: C0003259 / Source: MSH

Descendant Path 2 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Antigenic Variation CUI: C0003319 / Source: MSH
  3. Antigenic Drift and Shift CUI: C5544391 / Source: MSH

Descendant Path 3 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Aneuploidy CUI: C0002938 / Source: MSH
  5. Monosomy CUI: C0026499 / Source: MSH
  6. Chromosome Deletion CUI: C0008628 / Source: MSH

Descendant Path 4 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Aneuploidy CUI: C0002938 / Source: MSH
  5. Trisomy CUI: C0041107 / Source: MSH

Descendant Path 5 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Aneuploidy CUI: C0002938 / Source: MSH
  5. Tetrasomy CUI: C0333689 / Source: MSH

Descendant Path 6 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Mosaicism CUI: C0026578 / Source: MSH

Descendant Path 7 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Nondisjunction, Genetic CUI: C0028303 / Source: MSH
  5. Uniparental Disomy CUI: C0949628 / Source: MSH

Descendant Path 8 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Polyploidy CUI: C0032578 / Source: MSH
  5. Tetraploidy CUI: C0333694 / Source: MSH

Descendant Path 9 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Polyploidy CUI: C0032578 / Source: MSH
  5. Triploidy CUI: C0333693 / Source: MSH

Descendant Path 10 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Ring Chromosomes CUI: C0035639 / Source: MSH

Descendant Path 11 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Isochromosomes CUI: C0242621 / Source: MSH

Descendant Path 12 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromosome Breakage CUI: C0376628 / Source: MSH

Descendant Path 13 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromosome Inversion CUI: C0021943 / Source: MSH

Descendant Path 14 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromosome Duplication CUI: C1516516 / Source: MSH
  5. Trisomy CUI: C0041107 / Source: MSH

Descendant Path 15 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromosome Duplication CUI: C1516516 / Source: MSH
  5. Tetrasomy CUI: C0333689 / Source: MSH

Descendant Path 16 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Abnormal Karyotype CUI: C0476431 / Source: MSH
  5. XYY Karyotype CUI: C0043379 / Source: MSH

Descendant Path 17 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Sex Chromosome Aberrations CUI: C0036868 / Source: MSH
  5. XYY Karyotype CUI: C0043379 / Source: MSH

Descendant Path 18 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Uniparental Disomy CUI: C0949628 / Source: MSH

Descendant Path 19 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromothripsis CUI: C4277538 / Source: MSH

Descendant Path 20 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chromosomal Instability CUI: C1257806 / Source: MSH
  5. Chromosome Fragility CUI: C0008629 / Source: MSH

Descendant Path 21 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Chimerism CUI: C0333678 / Source: MSH

Descendant Path 22 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Micronuclei, Chromosome-Defective CUI: C1449861 / Source: MSH

Descendant Path 23 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Chromosome Aberrations CUI: C0008625 / Source: MSH
  4. Translocation, Genetic CUI: C0040715 / Source: MSH
  5. Philadelphia Chromosome CUI: C0031526 / Source: MSH

Descendant Path 24 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Frameshift Mutation CUI: C0079380 / Source: MSH

Descendant Path 25 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Gene Amplification CUI: C0017256 / Source: MSH

Descendant Path 26 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Gene Duplication CUI: C0017261 / Source: MSH

Descendant Path 27 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Mutagenesis, Insertional CUI: C0079868 / Source: MSH

Descendant Path 28 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Suppression, Genetic CUI: C0038855 / Source: MSH

Descendant Path 29 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Point Mutation CUI: C0162735 / Source: MSH

Descendant Path 30 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Sequence Deletion CUI: C0162773 / Source: MSH
  4. Chromosome Deletion CUI: C0008628 / Source: MSH

Descendant Path 31 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Sequence Deletion CUI: C0162773 / Source: MSH
  4. Gene Deletion CUI: C0017260 / Source: MSH

Descendant Path 32 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Germ-Line Mutation CUI: C0206530 / Source: MSH

Descendant Path 33 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Codon, Nonsense CUI: C0242612 / Source: MSH

Descendant Path 34 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. INDEL Mutation CUI: C1956002 / Source: MSH

Descendant Path 35 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Base Pair Mismatch CUI: C0600501 / Source: MSH

Descendant Path 36 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Mutation, Missense CUI: C0599155 / Source: MSH

Descendant Path 37 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Sequence Inversion CUI: C2718060 / Source: MSH
  4. Chromosome Inversion CUI: C0021943 / Source: MSH

Descendant Path 38 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Allelic Imbalance CUI: C0887935 / Source: MSH
  4. Loss of Heterozygosity CUI: C0524869 / Source: MSH
  5. Chromosome Deletion CUI: C0008628 / Source: MSH

Descendant Path 39 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Allelic Imbalance CUI: C0887935 / Source: MSH
  4. Loss of Heterozygosity CUI: C0524869 / Source: MSH
  5. Haploinsufficiency CUI: C2936267 / Source: MSH

Descendant Path 40 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Mutation Rate CUI: C3178846 / Source: MSH

Descendant Path 41 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Mutation Accumulation CUI: C4042934 / Source: MSH

Descendant Path 42 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Silent Mutation CUI: C1519323 / Source: MSH

Descendant Path 43 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Synthetic Lethal Mutations CUI: C4277595 / Source: MSH

Descendant Path 44 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Genomic Instability CUI: C0919532 / Source: MSH
  4. Microsatellite Instability CUI: C0920269 / Source: MSH

Descendant Path 45 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Genomic Instability CUI: C0919532 / Source: MSH
  4. Chromosomal Instability CUI: C1257806 / Source: MSH
  5. Chromosome Fragility CUI: C0008629 / Source: MSH

Descendant Path 46 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. DNA Repeat Expansion CUI: C1257790 / Source: MSH
  4. Trinucleotide Repeat Expansion CUI: C0524894 / Source: MSH

Descendant Path 47 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Loss of Function Mutation CUI: C4505106 / Source: MSH

Descendant Path 48 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Mutation CUI: C0026882 / Source: MSH
  3. Gain of Function Mutation CUI: C4505109 / Source: MSH

Descendant Path 49 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Genetic Heterogeneity CUI: C0242960 / Source: MSH

Descendant Path 50 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Quasispecies CUI: C4505259 / Source: MSH

Descendant Path 51 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Heteroplasmy CUI: C5392226 / Source: MSH

Descendant Path 52 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Phase Variation CUI: C5544526 / Source: MSH

Descendant Path 53 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Polymorphism, Genetic CUI: C0032529 / Source: MSH
  3. Polymorphism, Restriction Fragment Length CUI: C0035268 / Source: MSH

Descendant Path 54 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Polymorphism, Genetic CUI: C0032529 / Source: MSH
  3. Polymorphism, Single-Stranded Conformational CUI: C0243031 / Source: MSH

Descendant Path 55 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Polymorphism, Genetic CUI: C0032529 / Source: MSH
  3. Polymorphism, Single Nucleotide CUI: C0752046 / Source: MSH

Descendant Path 56 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Polymorphism, Genetic CUI: C0032529 / Source: MSH
  3. Genomic Structural Variation CUI: C2717924 / Source: MSH
  4. DNA Copy Number Variations CUI: C2717925 / Source: MSH

Descendant Path 57 (Top Source: MSH)

  1. Genetic Variation (START) CUI: C0042333 / Source: MSH
  2. Polymorphism, Genetic CUI: C0032529 / Source: MSH
  3. Pharmacogenomic Variants CUI: C4277630 / Source: MSH

Unique Ancestor Paths Found: 1 | Unique Descendant Paths Found: 57 | Max Depth: 10 levels.